---
title: "Ventriculostomy Kit, REF: 46154 — FDA record Z-2768-2026 | Is It on Recall"
description: "Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptabl"
url: https://isitonrecall.com/recall/fda-device-z-2768-2026-ventriculostomy-kit-ref-46154/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Ventriculostomy Kit, REF: 46154 — FDA record Z-2768-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 17, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Ventriculostomy Kit, REF: 46154
- **Reason**: Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices that come into contact with cerebrospinal fluid; endotoxin exposure can cause an acute inflammatory process.
- **Classification**: Class II
- **Recalling firm**: Medtronic Neurosurgery
- **Quantity**: 167
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2768-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2768-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 00673978947396, Lot: 2025-08779 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution in the states of UT, AL, CA, NC, GA, AR, LA, KY, LA, KY, IL, OK and the country of Costa Rica.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jul 29, 2026
- **Recall initiation date**: Jun 17, 2026
- **Center classification date**: Jul 21, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2768-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic Neurosurgery records](https://isitonrecall.com/brand/medtronic-neurosurgery/)